| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45396521C>T | CA359705203 | HCN1 | c.1201G>A (p.Asp401Asn) n.364G>A | ClinVar dbSNP COSMIC |
| 5 | g.45396521C>G | CA163271 | HCN1 | c.1201G>C (p.Asp401His) n.364G>C | ClinVar dbSNP |
| 5 | g.45396521C= | CA1543652919 | HCN1 | c.1201G= (p.Asp401=) n.364G= | dbSNP |